Skip to content

PEP uP Protocol in Surgical Patients

PEP uP Protocol (Enhanced Protein-Energy Provision Via the Enteral roUte Feeding Protocol) in Surgical Patients

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02459275
Enrollment
36
Registered
2015-06-02
Start date
2015-07-31
Completion date
2017-09-30
Last updated
2020-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critically Ill

Keywords

feeding protocol, enteral nutrition protocol, critically ill, surgical ICU, enteral nutrition, nutrition therapy

Brief summary

The main objective of this project is to asses for safety, feasibility and effectiveness of an aggressive feeding protocol, PEP uP (Enhanced Protein-Energy Provision via the Enteral Route Feeding Protocol) in increasing protein and energy delivery to critically ill surgical patients. Our hypothesis is that an aggressive feeding protocol, PEP uP will be safe, acceptable, and effectively increase protein and energy delivery to critically ill surgical patients.

Detailed description

Gross underfeeding or iatrogenic malnutrition is prevalent in intensive care units throughout the world. Critically ill patients only receive, on average, 40-50% of their prescribed nutritional requirements. Inadequate provision of nutrition to these patients is associated with increased complications, prolonged length of stay in the ICU and hospital, and increased mortality. There are good data from large scale observational studies and randomized trials that suggest better fed patients have better clinical and economic outcomes and there are ICUs that consistently reach an average of 80-90% nutritional adequacy (amount of nutrition received over amount prescribed) thus it appears to be a feasible goal. The PEP uP protocol (Enhanced Protein-Energy Provision via the Enteral Route Feeding Protocol) includes a new, innovative approach that protocolizes an aggressive set of strategies to providing enteral nutrition (EN) and shifts the paradigm from reactionary to proactive followed by de-escalation if nutrition therapy is not needed. The key components of this new PEP uP protocol are the following: 1. Starting feeds at the target rate based on increasing evidence that some patients tolerate starting nutrition at a higher rate of delivery and that slow start ups are not necessary. 2. Allowing trophic feeds a low volume of a concentrated feeding solution for 24 hours or longer, designed to maintain gastrointestinal structure and function for those patients who are deemed unsuitable for high volume intragastric feeds. 3. Prescribing semi-elemental feeding solution instead of a standard polymeric solution. These can then be changed to more traditional polymeric solution once the patient is tolerating adequate amounts of nutrition. 4. Prescribing protein supplements at initiation of EN and then discontinue if EN is well tolerated and protein requirement are met through their standard EN. 5. Starting motility agents at the same time EN is started with a re-evaluation in the days following to see if it is necessary. This PEP uP protocol has been previously studied in two published studies enrolling primarily medical patients. In the first study, a pilot before and after trial, the protocol seemed to be feasible, safe, and acceptable to critical care nurses. No incidents compromising patient safety were observed. (Heyland 2010) Rates of vomiting, regurgitation, aspiration, and pneumonia were similar and the PEP uP group received significantly more energy and protein (when they were prescribed to receive full volume as opposed to trophic). A subsequent multi-center cluster randomized trial involving low-performing ICUs likewise demonstrated that intervention sites had improvements in energy and protein delivery as well as a decrease in average time from ICU admission to start of enteral nutrition compared to the control group. (Heyland 2013).

Interventions

Semi-elemental tube feeds are started at the hourly goal rate as determined by the 24 hour volume goal. Protein supplements will be started at the initiation of tube feeds to target a daily delivery of 2 g/kg/day.

DRUGMetoclopramide

Metoclopramide 10mg Intravenous (IV) every 6 hours (q6h) or 5mg IV q6h for renal failure will be started empirically concomitant with EN initiation. Gastric Residual Volume (GRV) will be checked every 4 hours and will be reinfused to the patient each time it is checked.

Sponsors

Nestle Health Science
CollaboratorINDUSTRY
Clinical Evaluation Research Unit at Kingston General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * ICU admission within past 48 hours * Initiation of tube feeds currently planned by the surgical ICU (SICU) team and primary surgical team * Admitted by a surgical service to the SICU (not a medical ICU or neurology patient) * Expected to remain mechanically ventilated for \> 24 h and expected to require ICU care for \> 72 h after screening

Exclusion criteria

* Pregnancy * Attending surgeon preference (they must agree to feeding their patient according to the protocol in either arm using the goal rate determined by the SICU team and the nutritionist) * Contraindication to enteral nutrition (bowel obstruction, bowel discontinuity, proximal enterocutaneous fistula, and short gut syndrome) * Do not resuscitate (DNR) status or goals of care that specify limitations in medical therapies * Death expected within 24 hours

Design outcomes

Primary

MeasureTime frameDescription
Total Amount of Protein Received12 daysThe total amount of protein received from either EN or parenteral nutrition (PN), inclusive of propofol, divided by the amount prescribed as per the baseline assessment and expressed as a percentage.
Total Amount of Energy12 daysThe total amount of energy received from either EN or parenteral nutrition (PN), inclusive of propofol, divided by the amount prescribed as per the baseline assessment and expressed as a percentage.

Secondary

MeasureTime frameDescription
Time to Initiation of Enteral Nutrition12 daysHours from intensive care unit (ICU) admission
ICU Length of Stayup to 60 daysDays in the intensive care unit
Mortalityup to 60 daysNumber of participants that died
Hospital Length of Stayup to 60 daysDays the participants were in the admitted in the hospital

Countries

United States

Participant flow

Participants by arm

ArmCount
PEP uP Protocol
Participants will receive the PEP uP protocol with the pro motility agent. The intervention will be provided until the tube feeds are stopped or patient is fed meals orally and will be tracked until hospital discharge or 60 days which ever occur first. PEP uP Protocol: Semi-elemental tube feeds are started at the hourly goal rate as determined by the 24 hour volume goal. Protein supplements will be started at the initiation of tube feeds to target a daily delivery of 2 g/kg/day. Metoclopramide: Metoclopramide 10mg Intravenous (IV) every 6 hours (q6h) or 5mg IV q6h for renal failure will be started empirically concomitant with EN initiation. Gastric Residual Volume (GRV) will be checked every 4 hours and will be reinfused to the patient each time it is checked.
19
Standard of Care
Standard formula polymeric tube feeds started at a rate of 20 ml/hour. Gastric residual volume (GRV) will be checked every 4 hours. GRV is reinfused to the patient each time it is checked. GRV threshold is 200-500 ml. If the patient is tolerating tube feeds as determined by measuring the GRV, the rate is advanced by 20 ml/hour every 4 hours up to the goal rate. Participants will be followed until the tube feeds are stopped or patient is fed meals orally and will be tracked until hospital discharge or 60 days which ever occur first.
17
Total36

Baseline characteristics

CharacteristicPEP uP ProtocolStandard of CareTotal
Age, Continuous49.1 Years
STANDARD_DEVIATION 24.7
50.6 Years
STANDARD_DEVIATION 15.6
49.8 Years
STANDARD_DEVIATION 0.75
Race and Ethnicity Not Collected0 Participants
Sex: Female, Male
Female
1 Participants5 Participants6 Participants
Sex: Female, Male
Male
18 Participants12 Participants30 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
1 / 192 / 17
other
Total, other adverse events
0 / 190 / 17
serious
Total, serious adverse events
1 / 190 / 17

Outcome results

Primary

Total Amount of Energy

The total amount of energy received from either EN or parenteral nutrition (PN), inclusive of propofol, divided by the amount prescribed as per the baseline assessment and expressed as a percentage.

Time frame: 12 days

ArmMeasureValue (MEAN)Dispersion
PEP uP ProtocolTotal Amount of Energy49.4 percentage of energyStandard Deviation 23.7
Standard of CareTotal Amount of Energy60.3 percentage of energyStandard Deviation 22.8
Primary

Total Amount of Protein Received

The total amount of protein received from either EN or parenteral nutrition (PN), inclusive of propofol, divided by the amount prescribed as per the baseline assessment and expressed as a percentage.

Time frame: 12 days

ArmMeasureValue (MEAN)Dispersion
PEP uP ProtocolTotal Amount of Protein Received55.1 percentage of proteinStandard Deviation 24.4
Standard of CareTotal Amount of Protein Received52.9 percentage of proteinStandard Deviation 23.2
Secondary

Hospital Length of Stay

Days the participants were in the admitted in the hospital

Time frame: up to 60 days

ArmMeasureValue (MEAN)
PEP uP ProtocolHospital Length of Stay21.4 days
Standard of CareHospital Length of Stay16.6 days
Secondary

ICU Length of Stay

Days in the intensive care unit

Time frame: up to 60 days

ArmMeasureValue (MEAN)
PEP uP ProtocolICU Length of Stay12 days
Standard of CareICU Length of Stay12.5 days
Secondary

Mortality

Number of participants that died

Time frame: up to 60 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
PEP uP ProtocolMortality1 Participants
Standard of CareMortality2 Participants
Secondary

Time to Initiation of Enteral Nutrition

Hours from intensive care unit (ICU) admission

Time frame: 12 days

ArmMeasureValue (MEAN)
PEP uP ProtocolTime to Initiation of Enteral Nutrition26.7 hours
Standard of CareTime to Initiation of Enteral Nutrition28.2 hours

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026